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Neuropathology of JC virus infection in progressive multifocal leukoencephalopathy in remission

机译:进行性多灶性白质脑病缓解期JC病毒感染的神经病理学

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摘要

AIM: To investigate the neuropathology of the brain in a rare case of remission following diagnosis of progressive multifocal leukoencephalopathy (PML).METHODS: Consent from the family for an autopsy was obtained, clinical records and radiograms were retrieved. A complete autopsy was performed, with brain examination after fixation and coronal sectioning at 1 cm intervals. Fourteen regions were collected for paraffin embedding and staining for microscopic analysis. Histologic sections were stained with Luxol blue, hematoxylin/eosin, and immunostained for myelin basic protein, neurofilament, SV40 T antigen and p53. The biopsy material was also retrieved and sections were stained with hematoxylin/eosin and immunostained for SV40 and p53. Sections were examined by American Board of Pathology certified pathologists and images captured digitally.RESULTS: Review of the clinical records was notable for a history of ulcerative colitis resulting in total colectomy in 1977 and a liver transplant in 1998 followed by immune-suppressive therapy. Neurological symptoms presented immediately, therefore a biopsy was obtained which was diagnosed as PML. Immunotherapy was adjusted and clinical improvement was noted. No subsequent progression was reported. Review of the biopsy demonstrated atypical astrocytes and enlarged hyperchromatic oligodendroglial cells consistent with JC virus infection. Strong SV40 and p53 staining was found in glial cells and regions of dense macrophage infiltration were present. On gross examination of the post-mortem brain, a lesion in the same site as the original biopsy in the cerebellum was identified but no other lesions in the brain were found. Microscopic analysis of this cerebellar lesion revealed a loss of myelin and axons, and evidence of axonal damage. This single burned-out lesion was equivocally positive for SV40 antigen with little p53 staining. Examination of thirteen other brain regions found no other occult sites.CONCLUSION: Our study reveals residual damage, rare macrophages or other inflammation and minimal evidence of persistent virus. This case demonstrates the possibility of complete remission of PML.
机译:目的:研究在诊断为进行性多灶性白质脑病(PML)后极少见缓解的情况下大脑的神经病理学方法:方法:获得家属同意进行尸检,并取回临床记录和X光片。进行完整的尸检,在固定和冠状切片后每隔1 cm进行脑检查。收集十四个区域用于石蜡包埋和染色以进行显微镜分析。组织学切片用Luxol蓝,苏木精/曙红染色,并对髓鞘碱性蛋白,神经丝,SV40 T抗原和p53免疫染色。还取回活检材料,并将切片用苏木精/曙红染色,并对SV40和p53进行免疫染色。结果:经溃疡病性结肠炎病史回顾,1977年进行了全结肠切除术,1998年进行了肝移植,随后进行了免疫抑制治疗,对这些病史进行了回顾,对临床记录进行了回顾。立即出现神经系统症状,因此获得了被诊断为PML的活检。调整了免疫疗法并注意到临床改善。没有后续进展的报道。活检回顾显示,非典型星形胶质细胞和增大的增色性少突胶质细胞与JC病毒感染一致。在胶质细胞中发现强烈的SV40和p53染色,并且存在密集的巨噬细胞浸润区域。在对死后大脑进行大体检查时,发现了与小脑原始活检相同部位的病变,但未在大脑中发现其他病变。该小脑病变的显微镜分析显示髓鞘和轴突的损失,以及轴突损伤的证据。这个单一的烧毁病灶对SV40抗原含糊不清,几乎没有p53染色。对其他13个大脑区域的检查未发现其他隐匿部位。结论:我们的研究发现了残余损伤,罕见的巨噬细胞或其他炎症以及持续存在病毒的证据极少。这种情况证明了完全缓解PML的可能性。

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